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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1993856Generated: October 31, 2026

Sodium Hydroxide → HCID 66775751, compound

https://huagongshe.com/reaction/1993856

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant(2-(N-(tert-Butyl)sulfamoyl)-5-isobutylthiophen-3-yl)boronic acidHCID 11484000—
ReactantHCID 19043019HCID 19043019—
CatalystTriphenylphosphineHCID 11776—
Catalystpalladium(II) acetateHCID 167845—
SolventToluene ethanolHCID 21863594—
ProductHCID 66775751HCID 6677575166.6%

Reaction Conditions

Temperature80 °C

Reaction Steps

5-iso-Butyl-2-(N-tert-butylaminosulfonyl)thiophene-3-boronic acid (0.479 g, 1.5 mmol, see Example 1(c) above), 1-(4-bromobenzyl)-1H-[1,2,4]triazole (0.238 g, 1 mmol, see step (a) above), Pd(OAc)2 (15.7 mg, 0.03 mmol), triphenyl phosphine (15.7 mg, 0.06 mmol) and NaOH (0.16 g, 4 mmol) were dissolved in 4 mL of toluene/ethanol (4:1) in a thick walled glass tube, and were then heated to 80° C. for 1 h. The reaction mixture was cooled to rt, extracted with ethyl acetate and water and subsequently dried over K2CO3. The solvent was evaporated and the reaction mixture was separated on a silica column (dichloromethane+1% methanol to dichloromethane+4% methanol) to yield 0.288 g of the sub-title compound (65% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07652054B2
Source datasetuspto-grants-2010_01
ORD IDord-36ae5f5920d44c1d91628b05c637369f
Source noteuspto-grants-2010_01